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Pre-emptive product patentability declarations

机译:先发制品产品专利性声明

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摘要

Successful pharmaceutical products are typically protected by a number of patents (as well, potentially as other Intellectual property) directed toward specific aspects. Frequently, a product is initially patented in the form in which it was originally launched but then later modifications and improvements are also the subject of further patent applications. As readers will undoubtedly appreciate, prosecution of patent applications (whether for a new chemical entity or, as here, secondary applications of a drug) can take years to reach grant or rejection. Even then, European Opposition or US inter panes review proceedings may be brought, thereby extending the uncertainty as to the final form of claims. In consequence, potential producers of related products face a nearly impossible task in attempting to determine whether their own version will or will not infringe some yet-to-be examined application. Launching a product carries the uncomfortable risk that amendments to the claims of a pending application may result In the new product infringing.
机译:成功的药品通常受到针对特定方面的多项专利(以及其他知识产权)的保护。通常情况下,产品最初以最初发布的形式获得专利,但随后的修改和改进也是进一步专利申请的主题。读者无疑会理解,专利申请的起诉(无论是针对新的化学实体,还是像这里一样,针对药物的二次申请)可能需要数年时间才能获得批准或被拒绝。即便如此,欧洲的反对或美国的跨部门审查程序也可能被提起,从而扩大了索赔最终形式的不确定性。因此,相关产品的潜在生产商面临着一项几乎不可能完成的任务,即试图确定他们自己的版本是否会侵犯一些尚待审查的应用程序。发布产品会带来令人不安的风险,即对未决申请的索赔进行修改可能会导致新产品侵权。

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